Complete Up To Date Information about Liquisone F with Cerumene.
NADA Number: 032-322 | |
| Proprietary Name |
Liquisone F with Cerumene |
|---|---|
| Sponsor |
Evsco Pharmaceuticals, An Affiliate of IGI, Inc. |
| Sponsor Address |
Box 209 Harding Hwy. Buena, NJ 08310 USA |
| Ingredients |
Hexamethyltetracosane Prednisolone Tetracaine Neomycin Sulfate |
| Species |
Cat, no use class stated or implied Dog, no use class stated or implied |
| Routes of Administration |
Topical |
| Dose Form |
Liquid (suspension) |
| Drug Form |
Liquid (suspension) |
| Dispensing Status |
RX |
|
Dosage Amount, Indications & Limitations |
524.1484k Neomycin sulfate, prednisolone, tetracaine, and squalane topical-otic suspension. Specifications: Each milliliter of suspension contains 5 milligrams neomycin sulfate (equivalent to 3.5 milligrams neomycin base), 2 milligrams prednisolone, 5 milligrams tetracaine, and 0.25 milliliter squalane (hexamethyltetracosane). Conditions of use: Dogs Amount: 2 to 3 applications daily or as needed. Indications: For treating acute otitis externa and as adjunctive therapy in management of chronic otitis externa. Also for treating moist dermatitis in dogs. Limitations: Tetracaine and neomycin have the potential to sensitize. If signs of irritation or sensitivity develop, discontinue use. Prolonged use of this product may result in overgrowth of non-susceptible organisms. If new infections due to bacteria or fungi appear during therapy, appropriate measures should be taken. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Cats Amount: 2 to 3 applications daily or as needed. Indications: For treating acute otitis externa and as adjunctive therapy in management of chronic otitis externa. Limitations: Tetracaine and neomycin have the potential to sensitize. If signs of irritation or sensitivity develop, discontinue use. Prolonged use of this product may result in overgrowth of non-susceptible organisms. If new infections due to bacteria or fungi appear during therapy, appropriate measures should be taken. Federal law restricts this drug to use by or on the order of a licensed veterinarian. |
| Tolerances |
A tolerance of zero is established for residues of prednisolone in milk from dairy animals. Tolerances are established for residues of parent neomycin in uncooked edible tissues as follows: a. In cattle, swine, sheep, and goats: 7.2 parts per million in kidney (target tissue) and fat, 3.6 ppm in liver, and 1.2 ppm in muscle. b. In turkeys: 7.2 ppm in skin with adhering fat, 3.6 parts per million in liver, and 1.2 ppm in muscle. c. In milk: 0.15 part per million. |